David LeBlond, PhD
Biochemistry, M.S. Statistics
•CMC nonclinical and pre-clinical statistics. Process and analytical method development, optimization, validation, and comparability. Experimental design and analysis. Biosimilarity, Bio- & immuno-assays, Pharmaceutical Stability, dissolution, content uniformity, Compendial methods, QbD/Design space identification, measurement uncertainty, sample size determination, computer modeling and simulation, predictive analysis and risk assessment, Bayesian methods. Fluent in SAS, R, JMP, BUGS.
•Medical Device Diagnostics R&D and biometrics (17 years).
•Pharmaceutical Drug Development, non-clinical and pre-clinical statistics (16 years)
•CMC Statistical Consultant (2 years)
Other: Adjunct Instructor, University of Illinois College of Pharmacy, Biopharmaceutical Sciences. Member, USP Statistics Expert Committee, American Statistical Association, AAPS.
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